The Role of VHL in the Development of von Hippel-Lindau Disease and Erythrocytosis

Von Hippel-Lindau disease (VHL disease or VHL syndrome) is a familial multisystem neoplastic syndrome stemming from germline disease-associated variants of the VHL tumor suppressor gene on chromosome 3. VHL is involved, through the EPO-VHL-HIF signaling axis, in oxygen sensing and adaptive response...

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Detalles Bibliográficos
Autores principales: Hudler, Petra, Urbancic, Mojca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871608/
https://www.ncbi.nlm.nih.gov/pubmed/35205407
http://dx.doi.org/10.3390/genes13020362

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871608/
https://www.ncbi.nlm.nih.gov/pubmed/35205407
http://dx.doi.org/10.3390/genes13020362

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